Evidence map›Paper›PMID 26786778›Full record

ArticleAmerican journal of physiology. Endocrinology and metabolism2016

Neuregulin-1 attenuates development of nephropathy in a type 1 diabetes mouse model with high cardiovascular risk.

Leni Vandekerckhove, Zarha Vermeulen, Zhi Zhao Liu, Sonia Boimvaser, Andreas Patzak, Vincent F M Segers, Gilles W De Keulenaer

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Endocrinology and metabolism, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.0field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 44 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Natural Products in Renal-Associated Drug Discovery.Antioxidants (Basel, Switzerland) · 2023
    Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. The role of ErbB4 in cancer.Cellular oncology (Dordrecht, Netherlands) · 2020
    Review
  12. Article
  13. Article
  14. Article
  15. ErbB4 deletion accelerates renal fibrosis following renal injury.American journal of physiology. Renal physiology · 2018
    Article
  16. Article
  17. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 2 countries.

Leni VandekerckhoveLaboratory of Physiopharmacology, University of Antwerp, Wilrijk, Belgium; and.
Zarha VermeulenLaboratory of Physiopharmacology, University of Antwerp, Wilrijk, Belgium; and.
Zhi Zhao LiuAG Nierengefäßphysiologie, Institut für Vegetative Physiologie, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Sonia BoimvaserLaboratory of Physiopharmacology, University of Antwerp, Wilrijk, Belgium; and.
Andreas PatzakAG Nierengefäßphysiologie, Institut für Vegetative Physiologie, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Vincent F M SegersLaboratory of Physiopharmacology, University of Antwerp, Wilrijk, Belgium; and.
Gilles W De KeulenaerLaboratory of Physiopharmacology, University of Antwerp, Wilrijk, Belgium; and gilles.dekeulenaer@uantwerpen.be.
University of Antwerp · BECharité - Universitätsmedizin Berlin · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neuregulin-1 (NRG-1) is an endothelium-derived growth factor with cardioprotective and antiatherosclerotic properties and is currently being tested in clinical trials as a treatment for systolic heart failure. In clinical practice, heart failure often coexists with renal failure, sharing an overlapping pathophysiological background. In this study, we hypothesized that NRG-1 might protect against cardiomyopathy, atherosclerosis, and nephropathy within one disease process. We tested this hypothesis in a hypercholesterolemic apolipoprotein E-deficient (apoE(-/-)) type 1 diabetes mouse model prone to the development of cardiomyopathy, atherosclerosis, and nephropathy and compared the effects of NRG-1 with insulin. Upon onset of hyperglycemia induced by streptozotocin, apoE(-/-)mice were treated with vehicle, insulin, or recombinant human (rh)NRG-1 for 14 wk and were compared with nondiabetic apoE(-/-)littermates. Vehicle-treated diabetic apoE(-/-)mice developed left ventricular (LV) dilatation and dysfunction, dense atherosclerotic plaques, and signs of nephropathy. Nephropathy was characterized by abnormalities including hyperfiltration, albuminuria, increased urinary neutrophil gelatinase-associated lipocalin (NGAL), upregulation of renal fibrotic markers, and glomerulosclerosis. rhNRG-1 treatment induced systemic activation of ErbB2 and ErbB4 receptors in both heart and kidneys and prevented LV dilatation, improved LV contractile function, and reduced atherosclerotic plaque size. rhNRG-1 also significantly reduced albuminuria, NGALuria, glomerular fibrosis, and expression of fibrotic markers. Regarding the renal effects of rhNRG-1, further analysis showed that rhNRG-1 inhibited collagen synthesis of glomerular mesangial cells in vitro but did not affect AngII-induced vasoconstriction of glomerular arterioles. In conclusion, systemic administration of rhNRG-1 in hypercholesterolemic type 1 diabetic mice simultaneously protects against complications in the heart, arteries and kidneys.

Indexed as

AnimalsApolipoproteins EArteriolesCardiovascular DiseasesCollagenDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 1Diabetic NephropathiesDisease Models, AnimalErb-b2 Receptor Tyrosine KinasesHeartHeart VentriclesHypercholesterolemiaHypoglycemic AgentsInsulinKidneyApolipoproteins ECollagenErbb2 protein, mouseErb-b2 Receptor Tyrosine KinasesErbb4 protein, mouseHypoglycemic AgentsInsulinNeuregulin-1NRG1 protein, humanReceptor, ErbB-4Recombinant Proteinsatherosclerosisheart failurenephropathyneuregulin-1type 1 diabetes

Identifiers

PMID26786778
PMCPMC4824141
OpenAlexW2311397788

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.